Have questions? Visit https://www.reddit.com/r/SNPedia

rs387907005

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907005(G;G)
Make rs387907005(G;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40688643
GeneMAFB
is asnp
is mentioned by
dbSNPrs387907005
ebirs387907005
HLIrs387907005
Exacrs387907005
Varsomers387907005
Maprs387907005
PheGenIrs387907005
hapmaprs387907005
1000 genomesrs387907005
hgdprs387907005
ensemblrs387907005
gopubmedrs387907005
geneviewrs387907005
scholarrs387907005
googlers387907005
pharmgkbrs387907005
gwascentralrs387907005
openSNPrs387907005
23andMers387907005
23andMe allrs387907005
SNP Nexus

SNPshotrs387907005
SNPdbers387907005
MSV3drs387907005
GWAS Ctlgrs387907005
Max Magnitude0
ClinVar
Risk rs387907005(G;G)
Alt rs387907005(G;G)
Reference rs387907005(T;T)
Significance Pathogenic
Disease Multicentric osteolysis nephropathy
Variation info
Gene MAFB
CLNDBN Multicentric osteolysis nephropathy
Reversed 1
HGVS NC_000020.10:g.39317283A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023748.2,